Linked Data
ClinVar Variation Id:
513939
ClinVar RCV Id:
RCV000600592
dbSNP Id:
rs1556445122
gnomAD v4:
X-111682301-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.111682301G>T , CM000685.2:g.111682301G>T | GRCh38 |
| NC_000023.10:g.110925529G>T , CM000685.1:g.110925529G>T | GRCh37 |
| NC_000023.9:g.110812185G>T | NCBI36 |
| NG_016238.1:g.6184G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000623622.2:c.244+7G>T | ENSP00000485624.2:n.244+7G>T | |
| ENST00000699748.1:c.*213+7G>T | ENSP00000514558.1:n.*213+7G>T | |
| ENST00000394780.8:c.244+7G>T MANE Select | ENSP00000378260.3:n.244+7G>T | |
| ENST00000636363.1:c.244+7G>T | ENSP00000490681.1:n.244+7G>T | |
| ENST00000251943.8:c.-69+7G>T | ENSP00000251943.4:n.-69+7G>T | |
| ENST00000371979.7:c.244+7G>T | ENSP00000361047.3:n.244+7G>T | |
| ENST00000394780.7:c.244+7G>T | ENSP00000378260.3:n.244+7G>T | |
| ENST00000436609.5:c.-69+7G>T | ENSP00000392990.2:n.-69+7G>T | |
| ENST00000468657.5:c.*213+7G>T | ENSP00000480638.2:n.*213+7G>T | |
| ENST00000470971.5:c.*8+7G>T | ENSP00000479424.2:n.*8+7G>T | |
| ENST00000471924.5:c.321+7G>T | ENSP00000484523.2:n.321+7G>T | |
| ENST00000473389.5:c.244+7G>T | ENSP00000480711.1:n.244+7G>T | |
| ENST00000482374.5:c.*109+7G>T | ENSP00000479632.1:n.*109+7G>T | |
| ENST00000482742.5:c.-69+7G>T | ENSP00000477513.1:n.-69+7G>T | |
| ENST00000486353.5:c.244+7G>T | ENSP00000426892.2:n.244+7G>T | |
| ENST00000487141.5:c.280+7G>T | ENSP00000478130.1:n.280+7G>T | |
| ENST00000489033.5:c.*154+66G>T | ENSP00000482257.2:n.*154+66G>T | |
| ENST00000492038.5:c.*8+7G>T | ENSP00000479483.1:n.*8+7G>T | |
| ENST00000495283.5:c.*109+7G>T | ENSP00000427093.3:n.*109+7G>T | |
| ENST00000610588.4:c.10+66G>T | ENSP00000479731.1:n.10+66G>T | |
| ENST00000621367.4:c.-69+7G>T | ENSP00000481509.1:n.-69+7G>T | |
| ENST00000622986.3:c.244+7G>T | ENSP00000485067.1:n.244+7G>T | |
| ENST00000622997.3:c.*213+7G>T | ENSP00000485420.1:n.*213+7G>T | |
| ENST00000623144.3:c.*213+7G>T | ENSP00000485279.1:n.*213+7G>T | |
| ENST00000623148.3:c.262+66G>T | ENSP00000485658.1:n.262+66G>T | |
| ENST00000623189.1:c.-69+7G>T | ENSP00000485392.1:n.-69+7G>T | |
| ENST00000623255.1:c.235+1G>T | ENSP00000485333.1:n.235+1G>T | |
| ENST00000624161.3:c.*8+7G>T | ENSP00000485181.1:n.*8+7G>T | |
| ENST00000624881.3:c.185+66G>T | ENSP00000485093.1:n.185+66G>T | |
| NM_001039210.3:c.185+66G>T | NP_001034299.3:n.185+66G>T | |
| NM_001099922.2:c.244+7G>T | NP_001093392.1:n.244+7G>T | |
| NM_001168385.1:c.244+7G>T | NP_001161857.1:n.244+7G>T | |
| NM_001257230.1:c.-69+7G>T | NP_001244159.1:n.-69+7G>T | |
| NM_001257231.1:c.10+66G>T | NP_001244160.1:n.10+66G>T | |
| NM_001257234.1:c.-69+7G>T | NP_001244163.1:n.-69+7G>T | |
| NM_001257235.1:c.-69+7G>T | NP_001244164.1:n.-69+7G>T | |
| NM_001257237.1:c.-69+7G>T | NP_001244166.1:n.-69+7G>T | |
| NM_001257239.1:c.-69+7G>T | NP_001244168.1:n.-69+7G>T | |
| NM_001257240.1:c.-69+7G>T | NP_001244169.1:n.-69+7G>T | |
| NM_001257241.1:c.10+66G>T | NP_001244170.1:n.10+66G>T | |
| NM_018466.4:c.244+7G>T | NP_060936.1:n.244+7G>T | |
| NR_033125.1:n.241+7G>T | ||
| XM_005262191.3:c.-69+7G>T | XP_005262248.1:n.-69+7G>T | |
| XM_006724693.2:c.244+7G>T | XP_006724756.1:n.244+7G>T | |
| XM_006724695.2:c.244+7G>T | XP_006724758.1:n.244+7G>T | |
| XM_006724697.2:c.-69+7G>T | XP_006724760.2:n.-69+7G>T | |
| XM_006724698.2:c.-69+7G>T | XP_006724761.2:n.-69+7G>T | |
| XM_011531028.1:c.244+7G>T | XP_011529330.1:n.244+7G>T | |
| XM_011531029.1:c.244+7G>T | XP_011529331.1:n.244+7G>T | |
| XM_011531030.1:c.244+7G>T | XP_011529332.1:n.244+7G>T | |
| XM_011531031.1:c.-69+7G>T | XP_011529333.1:n.-69+7G>T | |
| XM_011531032.1:c.-69+7G>T | XP_011529334.1:n.-69+7G>T | |
| XM_011531033.1:c.-69+7G>T | XP_011529335.1:n.-69+7G>T | |
| XR_938409.1:n.717+7G>T | ||
| NM_001039210.4:c.185+66G>T | NP_001034299.3:n.185+66G>T | |
| NM_001168385.2:c.244+7G>T | NP_001161857.1:n.244+7G>T | |
| NM_001257235.2:c.-69+7G>T | NP_001244164.1:n.-69+7G>T | |
| NM_001257239.2:c.-69+7G>T | NP_001244168.1:n.-69+7G>T | |
| NM_001257240.2:c.-69+7G>T | NP_001244169.1:n.-69+7G>T | |
| NM_001257241.2:c.10+66G>T | NP_001244170.1:n.10+66G>T | |
| NM_001324290.1:c.250+1G>T | NP_001311219.1:n.250+1G>T | |
| NM_001324291.1:c.-69+7G>T | NP_001311220.1:n.-69+7G>T | |
| NM_001324292.1:c.244+7G>T | NP_001311221.1:n.244+7G>T | |
| NM_001324293.1:c.-69+7G>T | NP_001311222.1:n.-69+7G>T | |
| NM_001324294.1:c.-69+7G>T | NP_001311223.1:n.-69+7G>T | |
| NM_018466.5:c.244+7G>T | NP_060936.1:n.244+7G>T | |
| NR_033125.2:n.241+7G>T | ||
| NR_136735.1:n.314+7G>T | ||
| NR_148693.1:n.345+7G>T | ||
| XM_006724693.3:c.244+7G>T | XP_006724756.1:n.244+7G>T | |
| XM_006724697.3:c.-69+7G>T | XP_006724760.2:n.-69+7G>T | |
| XM_006724698.3:c.-69+7G>T | XP_006724761.2:n.-69+7G>T | |
| XM_011531028.2:c.244+7G>T | XP_011529330.1:n.244+7G>T | |
| XM_011531030.2:c.244+7G>T | XP_011529332.1:n.244+7G>T | |
| XM_011531033.3:c.-69+7G>T | XP_011529335.1:n.-69+7G>T | |
| XM_017029846.1:c.244+7G>T | XP_016885335.1:n.244+7G>T | |
| XM_017029847.1:c.244+7G>T | XP_016885336.1:n.244+7G>T | |
| XM_017029848.1:c.244+7G>T | XP_016885337.1:n.244+7G>T | |
| XM_017029849.1:c.244+7G>T | XP_016885338.1:n.244+7G>T | |
| XM_017029850.2:c.244+7G>T | XP_016885339.1:n.244+7G>T | |
| XM_017029851.1:c.-467+7G>T | XP_016885340.1:n.-467+7G>T | |
| XM_024452449.1:c.244+7G>T | XP_024308217.1:n.244+7G>T | |
| XR_001755726.1:n.284+7G>T | ||
| XR_001755727.1:n.284+7G>T | ||
| XR_001755728.1:n.284+7G>T | ||
| NM_001039210.5:c.185+66G>T | NP_001034299.3:n.185+66G>T | |
| NM_001099922.3:c.244+7G>T MANE Select | NP_001093392.1:n.244+7G>T | |
| NM_001168385.3:c.244+7G>T | NP_001161857.1:n.244+7G>T | |
| NM_001257230.2:c.-69+7G>T | NP_001244159.1:n.-69+7G>T | |
| NM_001257235.3:c.-69+7G>T | NP_001244164.1:n.-69+7G>T | |
| NM_001257239.3:c.-69+7G>T | NP_001244168.1:n.-69+7G>T | |
| NM_001257240.3:c.-69+7G>T | NP_001244169.1:n.-69+7G>T | |
| NM_001257241.3:c.10+66G>T | NP_001244170.1:n.10+66G>T | |
| NM_001324290.2:c.250+1G>T | NP_001311219.1:n.250+1G>T | |
| NM_001324291.2:c.-69+7G>T | NP_001311220.1:n.-69+7G>T | |
| NM_001324292.2:c.244+7G>T | NP_001311221.1:n.244+7G>T | |
| NM_001324294.2:c.-69+7G>T | NP_001311223.1:n.-69+7G>T | |
| NM_018466.6:c.244+7G>T | NP_060936.1:n.244+7G>T | |
| NR_033125.3:n.189+7G>T | ||
| NR_136735.2:n.314+7G>T | ||
| NR_148693.2:n.293+7G>T | ||
| NM_001257231.2:c.10+66G>T | NP_001244160.1:n.10+66G>T | |
| NM_001257234.2:c.-69+7G>T | NP_001244163.1:n.-69+7G>T | |
| NM_001257237.2:c.-69+7G>T | NP_001244166.1:n.-69+7G>T |